WO1996021655A3 - Inhibiteurs de la calpaine et/ou de la cathepsine b derives d'oxazolidine substituee - Google Patents

Inhibiteurs de la calpaine et/ou de la cathepsine b derives d'oxazolidine substituee Download PDF

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Publication number
WO1996021655A3
WO1996021655A3 PCT/US1995/016565 US9516565W WO9621655A3 WO 1996021655 A3 WO1996021655 A3 WO 1996021655A3 US 9516565 W US9516565 W US 9516565W WO 9621655 A3 WO9621655 A3 WO 9621655A3
Authority
WO
WIPO (PCT)
Prior art keywords
calpain
cathepsin
inhibitors
substituted oxazolidine
oxazolidine
Prior art date
Application number
PCT/US1995/016565
Other languages
English (en)
Other versions
WO1996021655A2 (fr
Inventor
Norton P Peet
Shujaath Mehdi
Matthew D Linnik
Michael R Angelastro
Hwa-Ok Kim
Original Assignee
Hoechst Marion Roussel Inc
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Priority to AT95943478T priority Critical patent/ATE206413T1/de
Priority to SI9530539T priority patent/SI0802909T1/xx
Priority to CA002210258A priority patent/CA2210258C/fr
Priority to DK95943478T priority patent/DK0802909T3/da
Priority to DE69523072T priority patent/DE69523072T2/de
Priority to MX9705235A priority patent/MX9705235A/es
Priority to NZ298999A priority patent/NZ298999A/xx
Priority to AU44731/96A priority patent/AU692044B2/en
Application filed by Hoechst Marion Roussel Inc filed Critical Hoechst Marion Roussel Inc
Priority to JP52166996A priority patent/JP4157601B2/ja
Priority to EP95943478A priority patent/EP0802909B1/fr
Publication of WO1996021655A2 publication Critical patent/WO1996021655A2/fr
Publication of WO1996021655A3 publication Critical patent/WO1996021655A3/fr
Priority to NO973216A priority patent/NO309267B1/no
Priority to FI972935A priority patent/FI972935A/fi

Links

Classifications

    • C—CHEMISTRY; METALLURGY
    • C07—ORGANIC CHEMISTRY
    • C07D—HETEROCYCLIC COMPOUNDS
    • C07D263/00—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings
    • C07D263/02—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings
    • C07D263/04—Heterocyclic compounds containing 1,3-oxazole or hydrogenated 1,3-oxazole rings not condensed with other rings having no double bonds between ring members or between ring members and non-ring members
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00—Drugs for disorders of the nervous system
    • A61P25/28—Drugs for disorders of the nervous system for treating neurodegenerative disorders of the central nervous system, e.g. nootropic agents, cognition enhancers, drugs for treating Alzheimer's disease or other forms of dementia
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00—Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/08—Vasodilators for multiple indications
    • A—HUMAN NECESSITIES
    • A61—MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61P—SPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P9/00—Drugs for disorders of the cardiovascular system
    • A61P9/10—Drugs for disorders of the cardiovascular system for treating ischaemic or atherosclerotic diseases, e.g. antianginal drugs, coronary vasodilators, drugs for myocardial infarction, retinopathy, cerebrovascula insufficiency, renal arteriosclerosis

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Veterinary Medicine (AREA)
  • General Chemical & Material Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Public Health (AREA)
  • Animal Behavior & Ethology (AREA)
  • General Health & Medical Sciences (AREA)
  • Biomedical Technology (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Cardiology (AREA)
  • Heart & Thoracic Surgery (AREA)
  • Urology & Nephrology (AREA)
  • Vascular Medicine (AREA)
  • Hospice & Palliative Care (AREA)
  • Psychiatry (AREA)
  • Heterocyclic Carbon Compounds Containing A Hetero Ring Having Nitrogen And Oxygen As The Only Ring Hetero Atoms (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)

Abstract

La présente invention concerne des inhibiteurs de la calpaïne et/ou de la cathepsine B dérivés d'oxazolidine et des compositions les renfermant. En tant qu'inhibiteurs de la calpaïne et/ou de la cathepsine B, ces composés sont utiles dans le traitement de patients souffrant de troubles neurodégénératifs aigus ou chroniques.
PCT/US1995/016565 1995-01-11 1995-12-15 Inhibiteurs de la calpaine et/ou de la cathepsine b derives d'oxazolidine substituee WO1996021655A2 (fr)

Priority Applications (12)

Application Number Priority Date Filing Date Title
NZ298999A NZ298999A (en) 1995-01-11 1995-12-15 4-benzyl-5-hydroxyoxazole derivatives acylated in position-1 by an amino acid, a dipeptide or an acyl group
CA002210258A CA2210258C (fr) 1995-01-11 1995-12-15 Inhibiteurs de la calpaine et/ou de la cathepsine b derives d'oxazolidine substituee
DK95943478T DK0802909T3 (da) 1995-01-11 1995-12-15 Substituerede oxazolidiner som calpain- og/eller cathepsin B-inhibitorer
DE69523072T DE69523072T2 (de) 1995-01-11 1995-12-15 Substituierte oxazolidine als calpain und/oder cathepsin b-hemmer
MX9705235A MX9705235A (es) 1995-01-11 1995-12-15 Inhibidores de calpaina y/o catepsina b de oxazolidina substituida.
AT95943478T ATE206413T1 (de) 1995-01-11 1995-12-15 Substituierte oxazolidine als calpain und/oder cathepsin b-hemmer
AU44731/96A AU692044B2 (en) 1995-01-11 1995-12-15 Substituted oxazolidine calpain and/or cathepsin B inhibitors
SI9530539T SI0802909T1 (en) 1995-01-11 1995-12-15 Substituted oxazolidine calpain and/or cathepsin b inhibitors
JP52166996A JP4157601B2 (ja) 1995-01-11 1995-12-15 置換オキサゾリジンカルパインおよび／またはカテプシンｂ阻害剤
EP95943478A EP0802909B1 (fr) 1995-01-11 1995-12-15 Inhibiteurs de la calpaine et/ou de la cathepsine b derives d'oxazolidine substituee
NO973216A NO309267B1 (no) 1995-01-11 1997-07-10 Substituerte oxazolidin-calpain- og/eller cathepsin B- inhibitorer og farmasöytisk preparat inneholdende disse
FI972935A FI972935A (fi) 1995-01-11 1997-07-10 Kalpaiinin ja/tai katepsiini B:n substituoituja oksatsolidiiniestäjiä

Applications Claiming Priority (2)

Application Number Priority Date Filing Date Title
US37119295A 1995-01-11 1995-01-11
US08/371,192 1995-01-11

Publications (2)

Publication Number Publication Date
WO1996021655A2 WO1996021655A2 (fr) 1996-07-18
WO1996021655A3 true WO1996021655A3 (fr) 1996-09-06

Family

ID=23462894

Family Applications (1)

Application Number Title Priority Date Filing Date
PCT/US1995/016565 WO1996021655A2 (fr) 1995-01-11 1995-12-15 Inhibiteurs de la calpaine et/ou de la cathepsine b derives d'oxazolidine substituee

Country Status (23)

Country Link
US (1) US5691368A (fr)
EP (1) EP0802909B1 (fr)
JP (1) JP4157601B2 (fr)
KR (1) KR100393701B1 (fr)
CN (1) CN1088456C (fr)
AR (1) AR001787A1 (fr)
AT (1) ATE206413T1 (fr)
AU (1) AU692044B2 (fr)
CA (1) CA2210258C (fr)
DE (1) DE69523072T2 (fr)
DK (1) DK0802909T3 (fr)
ES (1) ES2165441T3 (fr)
FI (1) FI972935A (fr)
HU (1) HUT77649A (fr)
IL (1) IL116724A (fr)
MX (1) MX9705235A (fr)
NO (1) NO309267B1 (fr)
NZ (1) NZ298999A (fr)
PT (1) PT802909E (fr)
SI (1) SI0802909T1 (fr)
TW (1) TW454001B (fr)
WO (1) WO1996021655A2 (fr)
ZA (1) ZA96100B (fr)

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WO2000021550A2 (fr) * 1998-10-13 2000-04-20 President And Fellows Of Harvard College Methodes et compositions de traitement des maladies neurodegeneratives
CA2350133A1 (fr) * 1998-11-12 2000-05-18 Research Corporation Technologies, Inc. Traitement de tissus ischemiquement degrades
EP1159273A1 (fr) * 1999-03-02 2001-12-05 Boehringer Ingelheim Pharmaceuticals Inc. Composes utiles en tant qu'inhibiteurs reversibles de la cathepsine s
TW200404789A (en) * 1999-03-15 2004-04-01 Axys Pharm Inc Novel compounds and compositions as protease inhibitors
EP1516877A1 (fr) * 1999-03-15 2005-03-23 Axys Pharmaceuticals, Inc. Derivés d'amine comme inhibiteurs de protease
US6506733B1 (en) 1999-03-15 2003-01-14 Axys Pharmaceuticals, Inc. Compounds and compositions as protease inhibitors
US6420364B1 (en) 1999-09-13 2002-07-16 Boehringer Ingelheim Pharmaceuticals, Inc. Compound useful as reversible inhibitors of cysteine proteases
FR2800737B1 (fr) * 1999-11-05 2006-06-30 Sod Conseils Rech Applic Nouveaux composes heterocycliques et leur application a titre de medicaments
CA2389685C (fr) * 1999-11-05 2011-07-12 Societe De Conseils De Recherches Et D'applications Scientifiques (S.C.R) Nouveaux composes heterocycliques et leur application a titre de medicaments
CA2417744A1 (fr) * 2000-07-31 2002-02-07 The Regents Of The University Of California Modele pour la maladie d'alzheimer et autres maladies neurodegenerative
JP2004523506A (ja) 2000-12-22 2004-08-05 アクシス・ファーマシューティカルズ・インコーポレイテッド カテプシン阻害剤としての新規な化合物と組成物
US7030116B2 (en) 2000-12-22 2006-04-18 Aventis Pharmaceuticals Inc. Compounds and compositions as cathepsin inhibitors
MXPA04002282A (es) 2001-09-14 2005-03-07 Axis Pharmaceutical Inc Nuevos compuestos y preparaciones como inhibidores de la catepsina.
RU2004117877A (ru) 2001-11-14 2006-01-10 Авентис Фармасьютикалз Инк. (Us) Олигопептиды и композиции, содержащие их, в качестве ингибиторов катепсина s
WO2004084830A2 (fr) * 2003-03-21 2004-10-07 Buck Institute Méthode de traitement de la maladie d'alzheimer
US7384970B2 (en) * 2003-03-24 2008-06-10 Irm Llc Inhibitors of cathepsin S
US7109243B2 (en) * 2003-03-24 2006-09-19 Irm Llc Inhibitors of cathepsin S
WO2004089395A2 (fr) * 2003-04-01 2004-10-21 Aventis Pharmaceuticals Inc. Utilisation d'un inhibiteur de la cathepsine-s ou -b afin de traiter ou de prevenir les maladies pulmonaires obstructives chroniques
US7732162B2 (en) 2003-05-05 2010-06-08 Probiodrug Ag Inhibitors of glutaminyl cyclase for treating neurodegenerative diseases
US7173051B2 (en) * 2003-06-13 2007-02-06 Irm, Llc Inhibitors of cathepsin S
US7256207B2 (en) * 2003-08-20 2007-08-14 Irm Llc Inhibitors of cathepsin S
FR2863268B1 (fr) * 2003-12-09 2006-02-24 Sod Conseils Rech Applic Nouveaux derives du 2-hydroxytetrahydrofuranne et leur application a titre de medicaments
EP2089383B1 (fr) 2006-11-09 2015-09-16 Probiodrug AG Dérivés 3-hydr0xy-1,5-dihydr0-pyrr0l-2-one utiles en tant qu' inhibiteurs de la glutaminyl-cyclase dans le traitement des ulcères, du cancer et d'autres maladies
DK2091948T3 (da) 2006-11-30 2012-07-23 Probiodrug Ag Nye inhibitorer af glutaminylcyclase
CA2679446C (fr) 2007-03-01 2016-05-17 Probiodrug Ag Nouvelle utilisation d'inhibiteurs de la glutaminyl cyclase
US9656991B2 (en) 2007-04-18 2017-05-23 Probiodrug Ag Inhibitors of glutaminyl cyclase
CA2729780A1 (fr) * 2008-07-03 2010-01-07 University Of Massachusetts Procedes et compositions pour reduire une inflammation et traiter des troubles inflammatoires
MX2012002993A (es) 2009-09-11 2012-04-19 Probiodrug Ag Derivados heterociclicos como inhibidores de ciclasa glutaminilo.
WO2011107530A2 (fr) 2010-03-03 2011-09-09 Probiodrug Ag Nouveaux inhibiteurs
JP5688745B2 (ja) 2010-03-10 2015-03-25 プロビオドルグ エージー グルタミニルシクラーゼ（ｑｃ、ｅｃ２．３．２．５）の複素環阻害剤
EP2560953B1 (fr) 2010-04-21 2016-01-06 Probiodrug AG Inhibiteurs de glutaminyl cyclase
ES2570167T3 (es) 2011-03-16 2016-05-17 Probiodrug Ag Derivados de benzimidazol como inhibidores de glutaminil ciclasa
ES2812698T3 (es) 2017-09-29 2021-03-18 Probiodrug Ag Inhibidores de glutaminil ciclasa
WO2024018245A1 (fr) 2022-07-22 2024-01-25 INSERM (Institut National de la Santé et de la Recherche Médicale) Utilisation d'inhibiteurs de calpaïne pour le traitement de la maladie rénale diabétique

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Also Published As

Publication number Publication date
CA2210258A1 (fr) 1996-07-18
DE69523072D1 (en) 2001-11-08
FI972935A0 (fi) 1997-07-10
KR100393701B1 (ko) 2003-11-28
AU4473196A (en) 1996-07-31
EP0802909A2 (fr) 1997-10-29
DE69523072T2 (de) 2002-06-20
SI0802909T1 (en) 2002-02-28
AU692044B2 (en) 1998-05-28
IL116724A (en) 2000-08-31
CA2210258C (fr) 2002-10-01
DK0802909T3 (da) 2002-01-28
US5691368A (en) 1997-11-25
NO309267B1 (no) 2001-01-08
NZ298999A (en) 1999-01-28
CN1173174A (zh) 1998-02-11
NO973216L (no) 1997-09-09
NO973216D0 (no) 1997-07-10
JP4157601B2 (ja) 2008-10-01
WO1996021655A2 (fr) 1996-07-18
ES2165441T3 (es) 2002-03-16
FI972935A (fi) 1997-07-10
JPH10512257A (ja) 1998-11-24
TW454001B (en) 2001-09-11
IL116724A0 (en) 1996-05-14
ZA96100B (en) 1996-07-24
PT802909E (pt) 2002-03-28
EP0802909B1 (fr) 2001-10-04
HUT77649A (hu) 1998-07-28
ATE206413T1 (de) 2001-10-15
MX9705235A (es) 1997-10-31
CN1088456C (zh) 2002-07-31
AR001787A1 (es) 1997-12-10

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